4-Methyl-5-thiazolecarbaldehyde

COCc1scnc1C
Reaction #2900
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ncsc1C=CC(=O)C(C)C
Reaction #51720
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ncsc1C(O)c1cccc(N(C)C)c1
Reaction #177982
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCc1scnc1C
Reaction #178243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C(=O)C=Cc2scnc2C)ccc1O
Reaction #272335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ncsc1C(O)c1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c(N2C[C@@H](C)O[C@@H](C)C2)c(F)c1F
Reaction #332574
{5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-4-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-2,3-difluorophenyl}(4-methyl-1,3-thiazol-5-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)c1nc2n(c1C(O)c1scnc1C)CCOc1cc(F)c(Br)cc1-2
Reaction #662571
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1ncsc1C(O)c1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c(N2C[C@@H](C)O[C@@H](C)C2)c(F)c1F
Reaction #665028
{5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-4-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-2,3-difluorophenyl}(4-methyl-1,3-thiazol-5-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1ncsc1C(O)CC1CCCCC1
Reaction #738227
title compound
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
Cc1ncsc1C(O)CC1CCCCC1
Reaction #760905
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1ncsc1C(O)c1cccc(N(C)C)c1
Reaction #814435
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
COCc1scnc1C
Reaction #1062228
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
O=C(C=Cc1ccccc1)c1ccccc1
Reaction #1106627
chalcone
Rendement 5.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
Cc1ncsc1C(O)C(F)(F)F
Reaction #1273550
2,2,2-trifluoro-1-(4-methylthiazol-5-yl)ethanol
Rendement 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
Cc1ncsc1C(O)c1scnc1C
Reaction #1464736
bis(4-methyl-5-thiazolyl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
Cc1ncsc1C(O)c1cccc(N(C)C)c1
Reaction #1545405
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
Cc1ncsc1C=CC(=O)C(C)C
Reaction #1647323
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COc1ccc(C(=O)/C=C/c2scnc2C)cn1
Reaction #1705082
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1ncsc1C=CC(=O)C(C)C
Reaction #1946696
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
Cc1ncsc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #1991828
7-(phenoxyacetamido)-3-[2-(4-methylthiazol-5-yl)vinyl]-3-cephem-4-carboxylic acid benzhydryl ester
Rendement 59.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_06
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